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Clinical Trials/NCT04428970
NCT04428970CompletedNot Applicable

Intracranial Pressure Monitoring Following Traumatic Brain Injury - Evaluation of Indications, Complications, and Significance of Follow-up Imaging.

Medical University of Vienna1 site in 1 country214 target enrollmentStarted: January 1, 2007Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
214
Locations
1
Primary Endpoint
Complications

Study Overview

Brief Summary

The aim of this retrospective cohort study is to evaluate complications rates, indications, and the utility of follow-up imaging studies of ICP measurement in severe TBI patients.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Severe Traumatic Brain Injury (GCS<9 on arrival)
  • Implantation of invasive intracranial parenchymal ICP monitoring

Exclusion Criteria

  • incomplete data records

Outcomes

Primary Outcomes

Complications

Time Frame: up to 30 days

Intervention-related complications

Secondary Outcomes

  • Clinical outcome(up to 30 days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Thomas Haider

M.D., Ph.D.

Medical University of Vienna

Study Sites (1)

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